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Review: Benefits of antidepressants outweigh risks of suicidal ideation and attempts in children and adolescents.

机译:综述:抗抑郁药的益处超过了儿童和青少年自杀意念和尝试自杀的风险。

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In 2004, Hie FDA required a boxed warning for all antidepressant drugs regarding the increased risk of suicidal behaviour and ideation in children and adolescents based on an analysis of all available randomised, placebo-controlled trials (RCTs) of these drugs.1 Bridge and colleagues expanded this effort by re-examining this risk within the context of possible benefit. They collected data examining the use of antidepressant drugs across several indications. Although they used a slightly different subset of RCTs lhan previous FDA work, and a slightly different method for estimating risk, both reached a similar conclusion about the risk The contribution of the present paper is the estimates of benefit based on iheir metaanafysis of efficacy results. They concluded ihat efficacy "appears greatest for non-OCD anxiety disorders, iniermediate for.OCD, and more modest for MDD". Their quantification of risk and benefit in terms"bf NNH arid NKT is helpful in supporting their conclusion that the benefits outweigh the. risks across the range of disorders studied.The reported analysesare post hoc and caution is generally warranted in the interpretation of the findings. In addition, most of ihe RCTs are short term and thus cannot address longer-term benefits and risks. !t is, worth noting ihat adult maintenance trials wiifi antidepressants almost always show a benefit in maintaining treatment in responders. Furthermore, these data cannot provide valid comparisons between the individual drugs studied; some had smaller numbers of RCTs than others and consequently less of an opportunity to observe the risk or the benefit. Finally, dose effect was not explored.Although there remain differences of opinion about the reported risk and its implications for clinical practice, the evidence presented by Bridge and colleagues supports the FDA recommendations1 for ilie cautious and closely monitored use of antidepressant drugs in children and adolescents as a way to maximise me benefit and minimise the risk.
机译:2004年,Hie FDA根据对所有抗抑郁药的所有可用随机,安慰剂对照试验(RCT)进行的分析,要求所有抗抑郁药都应加框警告,以增加儿童和青少年自杀行为和意念的风险。1Bridge和同事通过在可能的收益范围内重新检查此风险来扩展此工作。他们收集了检查多种适应症的抗抑郁药使用情况的数据。尽管他们使用的RCT子集与之前的FDA工作相比略有不同,并且使用的风险评估方法也略有不同,但两者均得出了与风险相似的结论。本文的贡献是根据功效结果的荟萃分析估算收益。他们总结说,“非OCD焦虑症表现最强,OCD介导中等,MDD表现较弱”。他们用“ NHF NBT和NKT”来量化风险和收益,有助于支持他们得出的结论,即在所研究的各种疾病中收益大于风险。所报道的分析是事后进行的,在解释研究结果时通常应谨慎行事。此外,大多数随机对照试验都是短期的,因此不能解决长期获益和风险,值得一提的是,在成人抗抑郁试验中,使用抗抑郁药几乎总是显示出对应答者维持治疗的益处,而且,这些数据不能提供在所研究的各个药物之间进行了有效的比较;某些药物的RCT数量少于其他药物,因此观察风险或获益的机会较少;最后,并未探讨剂量效应。对于临床实践而言,Bridge及其同事提供的证据支持FDA对谨慎的建议并密切监控儿童和青少年使用抗抑郁药的方法,以最大程度地提高我的利益并最大程度地降低风险。

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